JPS6340194B2 - - Google Patents

Info

Publication number: JPS6340194B2
Authority: JP; Japan
Prior art keywords: formula; alkyl group; parts; represented; moisture
Prior art date: 1978-07-24
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

JP54089947A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5527179A (en

Inventor

Ansonii Seera Jeimusu

Dankan Mitsucheru Tairon

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

General Electric Co

Original Assignee

General Electric Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1978-07-24

Filing date

1979-07-17

Publication date

1988-08-10

1979-07-17 Application filed by General Electric Co filed Critical General Electric Co

1980-02-27 Publication of JPS5527179A publication Critical patent/JPS5527179A/ja

1988-08-10 Publication of JPS6340194B2 publication Critical patent/JPS6340194B2/ja

Status Granted legal-status Critical Current

Links

-1 aliphatic alcohols Chemical class 0.000 claims description 17
125000000217 alkyl group Chemical group 0.000 claims description 10
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 6
SURCGQGDUADKBL-UHFFFAOYSA-N 2-(2-hydroxyethylamino)-5-nitrobenzo[de]isoquinoline-1,3-dione Chemical compound [O-][N+](=O)C1=CC(C(N(NCCO)C2=O)=O)=C3C2=CC=CC3=C1 SURCGQGDUADKBL-UHFFFAOYSA-N 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
125000002947 alkylene group Chemical group 0.000 claims description 3
125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 2
238000004519 manufacturing process Methods 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims 2
239000002253 acid Substances 0.000 claims 1
125000005843 halogen group Chemical group 0.000 claims 1
239000000203 mixture Substances 0.000 description 17
229920001296 polysiloxane Polymers 0.000 description 12
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 7
125000003545 alkoxy group Chemical group 0.000 description 6
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical compound [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 6
238000000034 method Methods 0.000 description 6
JLUFWMXJHAVVNN-UHFFFAOYSA-N methyltrichlorosilane Chemical compound C[Si](Cl)(Cl)Cl JLUFWMXJHAVVNN-UHFFFAOYSA-N 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
239000005055 methyl trichlorosilane Substances 0.000 description 5
238000013008 moisture curing Methods 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
238000001723 curing Methods 0.000 description 3
125000004122 cyclic group Chemical group 0.000 description 3
BADXJIPKFRBFOT-UHFFFAOYSA-N dimedone Chemical compound CC1(C)CC(=O)CC(=O)C1 BADXJIPKFRBFOT-UHFFFAOYSA-N 0.000 description 3
239000004205 dimethyl polysiloxane Substances 0.000 description 3
150000002367 halogens Chemical class 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 3
MJKVTPMWOKAVMS-UHFFFAOYSA-N 3-hydroxy-1-benzopyran-2-one Chemical compound C1=CC=C2OC(=O)C(O)=CC2=C1 MJKVTPMWOKAVMS-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
230000000694 effects Effects 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
239000007788 liquid Substances 0.000 description 2
125000000962 organic group Chemical group 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
238000003756 stirring Methods 0.000 description 2
YCWRLBFFWYMHAQ-UHFFFAOYSA-N 1-phenylpyrrolidine-2,4-dione Chemical compound O=C1CC(=O)CN1C1=CC=CC=C1 YCWRLBFFWYMHAQ-UHFFFAOYSA-N 0.000 description 1
UBUJDMSDEQBNTG-UHFFFAOYSA-N 2-bromocyclohexane-1,3-dione Chemical compound BrC1C(=O)CCCC1=O UBUJDMSDEQBNTG-UHFFFAOYSA-N 0.000 description 1
HXZILEQYFQYQCE-UHFFFAOYSA-N 2-methylcyclopentane-1,3-dione Chemical compound CC1C(=O)CCC1=O HXZILEQYFQYQCE-UHFFFAOYSA-N 0.000 description 1
UMZODYOZUBWCCB-UHFFFAOYSA-N 6,6-dimethyloxane-2,4-dione Chemical compound CC1(C)CC(=O)CC(=O)O1 UMZODYOZUBWCCB-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000000732 arylene group Chemical group 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
125000000068 chlorophenyl group Chemical group 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000002993 cycloalkylene group Chemical group 0.000 description 1
125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
OILAIQUEIWYQPH-UHFFFAOYSA-N cyclohexane-1,2-dione Chemical compound O=C1CCCCC1=O OILAIQUEIWYQPH-UHFFFAOYSA-N 0.000 description 1
HJSLFCCWAKVHIW-UHFFFAOYSA-N cyclohexane-1,3-dione Chemical compound O=C1CCCC(=O)C1 HJSLFCCWAKVHIW-UHFFFAOYSA-N 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
230000007423 decrease Effects 0.000 description 1
238000010586 diagram Methods 0.000 description 1
239000012975 dibutyltin dilaurate Substances 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
239000000806 elastomer Substances 0.000 description 1
125000001033 ether group Chemical group 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
229910021485 fumed silica Inorganic materials 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
239000000463 material Substances 0.000 description 1
GXHFUVWIGNLZSC-UHFFFAOYSA-N meldrum's acid Chemical compound CC1(C)OC(=O)CC(=O)O1 GXHFUVWIGNLZSC-UHFFFAOYSA-N 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
230000009965 odorless effect Effects 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000000376 reactant Substances 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
229910052710 silicon Inorganic materials 0.000 description 1
239000010703 silicon Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
125000005023 xylyl group Chemical group 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/04—Esters of silicic acids
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/04—Esters of silicic acids
- C07F7/06—Esters of silicic acids with hydroxyaryl compounds

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)

JP8994779A 1978-07-24 1979-07-17 Carbonylsilylether Granted JPS5527179A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/927,287 US4238401A (en)	1978-07-24	1978-07-24	Alkoxysilicon materials and method for making

Publications (2)

Publication Number	Publication Date
JPS5527179A JPS5527179A (en)	1980-02-27
JPS6340194B2 true JPS6340194B2 (ru)	1988-08-10

Family

ID=25454521

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP8994779A Granted JPS5527179A (en)	1978-07-24	1979-07-17	Carbonylsilylether

Country Status (5)

Country	Link
US (1)	US4238401A (ru)
JP (1)	JPS5527179A (ru)
DE (1)	DE2929225A1 (ru)
FR (1)	FR2433531A1 (ru)
GB (1)	GB2026509B (ru)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4358575A (en) *	1981-12-16	1982-11-09	General Electric Company Silicone Products Business Division	Self-bonding one-component RTV silicone rubber compositions
US4395507A (en) *	1981-12-16	1983-07-26	General Electric Silicones	Self-bonding one-component dimedone RTV silicone rubber compositions
DE3377127D1 (en) *	1982-08-20	1988-07-28	Hoffmann La Roche	Process for the preparation of astaxanthine and intermediates in the astaxanthine synthesis
GB2130229A (en) *	1982-11-04	1984-05-31	Gen Electric	Dialkoxysilylenolethers and method for making them
FR2537142A1 (fr) *	1982-12-03	1984-06-08	Gen Electric	Ethers de dialcoxysilylenol et leur procede de preparation
US4804774A (en) *	1988-04-04	1989-02-14	Ethyl Corporation	Production of gem-disubstituted cyclohexadienones
US4845258A (en) *	1988-04-04	1989-07-04	Ethyl Corporation	Production of gem-disubstituted cyclohexadienones
US4804772A (en) *	1988-04-04	1989-02-14	Ethyl Corporation	Gem-disubstituted cyclohexadienones and their production
US4804773A (en) *	1988-04-04	1989-02-14	Ethyl Corporation	Production of gem-disubstituted cyclohexadienones
US5008425A (en) *	1988-04-04	1991-04-16	Ethyl Corporation	Trifluoromethylation of carbonyl compounds
FR2725207B1 (fr)	1994-09-30	1996-11-29	Exsymol Sa	Composes a base de silicium biologiquement actifs, leurs applications therapeutiques et cosmetiques
JPWO2023032745A1 (ru) *	2021-09-03	2023-03-09

1978
- 1978-07-24 US US05/927,287 patent/US4238401A/en not_active Expired - Lifetime
1979
- 1979-06-12 GB GB7920413A patent/GB2026509B/en not_active Expired
- 1979-07-17 JP JP8994779A patent/JPS5527179A/ja active Granted
- 1979-07-19 DE DE19792929225 patent/DE2929225A1/de not_active Withdrawn
- 1979-07-24 FR FR7919010A patent/FR2433531A1/fr active Granted

Also Published As

Publication number	Publication date
US4238401A (en)	1980-12-09
DE2929225A1 (de)	1980-02-14
FR2433531A1 (fr)	1980-03-14
FR2433531B1 (ru)	1984-06-22
GB2026509B (en)	1982-12-08
JPS5527179A (en)	1980-02-27
GB2026509A (en)	1980-02-06

Publication	Publication Date	Title
EP0629648B1 (en)	1998-07-08	Method for preparation of carbinol-functional siloxanes
JPS6340194B2 (ru)	1988-08-10
JPH06172536A (ja)	1994-06-21	室温硬化性シリコーンシーラント及びその製造方法
US5395955A (en)	1995-03-07	Method for the preparation of carbinol group-containing organopolysiloxane
JPH06172535A (ja)	1994-06-21	クラスターアザシラシクロアルキル官能性ポリシロキサンの調製方法
JPH01207294A (ja)	1989-08-21	含フッ素有機ケイ素化合物
JPS6340195B2 (ru)	1988-08-10
RU2230747C2 (ru)	2004-06-20	Новые фторалкилзамещенные циклотрисилоксаны, их использование для получения новых полимеров и новые полимеры
EP1149837A2 (en)	2001-10-31	Organosilicon compounds
JPS638146B2 (ru)	1988-02-20
US6060618A (en)	2000-05-09	Fluorine-containing amide compound
JP3915883B2 (ja)	2007-05-16	有機ケイ素化合物
JPS6155516B2 (ru)	1986-11-28
JPH07242678A (ja)	1995-09-19	２，４，６，８−テトラメチルシクロテトラシロキサンの製造方法
EP1233020B1 (en)	2005-04-13	Fluorinated organosilicon compounds
JPH06166690A (ja)	1994-06-14	含フッ素有機ケイ素化合物
JP4055429B2 (ja)	2008-03-05	含フッ素有機ケイ素化合物
JP2758116B2 (ja)	1998-05-28	メチル基含有ポリシランの製造方法
JPH06107671A (ja)	1994-04-19	有機ケイ素化合物及びその製造方法
CA1123849A (en)	1982-05-18	Alkoxysilicon materials and method for making
JP2016204287A (ja)	2016-12-08	加水分解性シリル基含有環状オルガノハイドロジェンシロキサン
JP3124910B2 (ja)	2001-01-15	シクロトリシロキサン及びその製造方法
JP3257414B2 (ja)	2002-02-18	環状エーテル基を有するオルガノポリシロキサン
JPH07309879A (ja)	1995-11-28	耐熱性ケイ素系高分子及びその製造方法、及び該高分子の製造に用いる有機ケイ素化合物
JPH0615618B2 (ja)	1994-03-02	含フッ素ポリシルエチレンシロキサン